List of variants in gene PRICKLE1 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_153026.3(PRICKLE1):c.649T>C (p.Cys217Arg)	rs772276749	0.00006
NM_153026.3(PRICKLE1):c.1942C>T (p.Arg648Trp)	rs370129051
NM_153026.3(PRICKLE1):c.2242A>G (p.Met748Val)
NM_153026.3(PRICKLE1):c.384+6C>A	rs764025084

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